Cyano substituted phenylhydrazones of 1 2-dicarbonyl compounds

ABSTRACT

A-(HALO, CYANO, NITRO AND AZIDO)-A-(ALKANOYL, CARBOALKOXY (I.E. ALKOXY CARBONYL), AMINO AND MONO- AND DIALKYL AMINO)-CARBONYL-(UNSUBSTITUTED AND MONO TO PENTA ALKY AND/OR ELECTROEGATIVE SUBSTITUENT (E.G. HALO, NITRO, CYANO, TRIFFUOROMETHYL, TRIFLUOROMETHYL-, -MERCAPTO, -SULFONYL AND -SULFOXYL, ALKOXY, ALKYL SUFONYL AND/OR DIMETHYLMINO SULFONYL)-SUBSTITUTED) PHENYLHYDRAZONES AND THEIR CORRESPONDING ALKALI METAL, ALKALINE EARTH METAL AND AMINE SALTS, WHICH POSSESS PEDTICIDAL, ESPECIALLY ACARICIDAL AND INSECTICDAL, PROPERTIES AND WHICH MAY BE PRODUCED BY CONVENTIONAL METHODS.

' 3,641,098 I CY NO SUBSTITUTED PHENYLHYDRAZONES F 4 1,2-DICARBONYL COMPOUNDS Karl-Heinz I Buchel and Wilfried Draber, Leverkusen,

Ingeborg Hammann, Cologne, and Gunter Unterstenhofer, Opladen, Germany, assignors to Farbenfabriken Bayer Aktiengesellschaft, Leverkusen, Germany v1-I0Drawing. Filed Sept. 24, 1968, Ser. No. 762,155

Claims priority, application Germany, Sept. 26, 1967,

P 16 68 225.4 Int. Cl. C07c 133/00 US; (11.260-465 6 Claims a ABSTRACT OF THE DISCLOSURE cr -(Halo, cyano, nitro and azido)-a-(alkanoyl, carboalkoxy [i.e. alkoxy carbonyl], amino and monoand dialkyl amino)-carbonyl-(unsubstituted and mono to penta alkyl and/or electronegative substituent [c.g. halo, nitro, cyano, trifluoromethyl, trifluoromethyl-, -mercapto, -sulfonyl and -sulfoxyl, alkoxy, alkylsulfonyl and/ or dimethylmino sulfonyH-substituted) phenyl hydrazones and their Corresponding alkali metal, alkaline earth metal and amine salts, which possess pesticidal, especially acaricidal and insecticidal, properties and which may be produced by conventionalmethods.

.The present invention relates to and has for its objects the provision for new phenylhyrazones of 1,2-dicarbonyl compounds, i.e. ot-substituted carbonyl-phenylhydrazones or N-(carbonyl-methyleneimino)-ani1ines, which possess pesticidal, especially insecticidal and acaricidal, properties, active compositions in the form of mixtures of such compounds with solid and liquid dispersible carrier vehicles, and methods for producing such compounds and for using such compounds in a new way especially for combating pests, e.g. arthropods, with other and further objects becoming apparent from a study of the within specification and accompanying examples. .It isalready known that certain phenylhydrazones of 'dicyanoketone, for example a,u-dicyano-carbonyl-2,5-dichlorophenylhydrazine (A) can be used for the control of insectsand mites (see US. Pat; 3,157,569).

It has been found in accordance with the present invention that the new phenylhydrazones of the formula Y NN=C Zm II ,i which 0 X is halogen, cyan, nitro or azido,

Y isQC alkyl, C 4 alkoxy or -NRR', R and R'are hydrogen or Ci alkyl,

"Z is (3 alkyl, alkoxy, or an electronegative substituent,

Q I Zm in which I a Z and m are the same as defined above and -strong 'pesticidal, especially insecticidal and acaricidal,

United-States Patent Q 3,641,098 Patented Feb. 8, 1972 A stands for an anion introduced by the diazotization, is reacted, optionally in the presence of a solvent, with an active methylene compound of the formula W o (11b) in which X and Y are the same as defined above, or

[b] a diazotization product of an amine according to Formula Ila above is reacted with a 2-halogen-l,3-dicar-' bonyl compound of the formula 011 0 0 Hal H J-Y (He) in which Y is the same as define above and Hal is halogen such as chloro, bromo, iodo, or fiuoro, optionally in the presence of a solvent,

Y, Z and m are the same as defined above and Hal is halgen such as chloro, bromo, iodo or fluoro, is reacted, optionally in the presence of a solvent, with an alkali metal salt of the formula Me X' (lid) in which Me is an alkali metal such as sodium, potassium or lithium, and

X is cyano, azido or nitro.

It is to be noted that the starting materials (I') of the process [c] can be prepared according to the processes [a] and [b], all of which are new compounds according to the present invention.

The term solvent as used herein includes mere diluents, as the artisan will appreciate.

It is surprising that the new phenylhydrazones according to the present invention exhibit a stronger insecticidal and acaricidal effectiveness than the chemically very similar previously known phenylhydrazones.

If 3,5-bis(trifiuoromethy1)aniline, which was diazotized in phosphoric acid with nitrosyl-sulfuric acid at 0-10 :C.,

and cyano-acetic acid methyl esterare used as starting materials, the reaction course of the process variant [a] can be represented by thefollowing equation:

Fae 9393 (IIaa) If 2 chloro trifluoromethyl aniline, which was diazotized in concentrated hydrochloric acid with NaNO and a-chloro-acetyl-acetone are used as starting materials, a phenylhydrazone according to the present invention is obtained which can be reacted for example with KCN, to give a further phenylhydrazone according to the present invention.

The reaction course according to process variants [b] and [c] is represented by the following over-all equation:

The starting materials (Ha), (IIb) and (He) used for process variants [a] and [b], as well as the starting materials (IId) used for process variant [0] are already known and can be prepared in simple manner according to known processes. The starting materials (I') used for process variant [c] are new compounds of the present invention and, of course, are obtained according to the process variants [a] and [b].

Advantageously, in accordance with the present invention, in the various formulae herein:

X represents:

Halo such as chloro, bromo, iodo and fluoro, especially chloro and bromo, and particularly chloro; cyano; nitro; or azido, i.e., -N;,;

Y represents:

Straight and branched chain alkyl having 1-4 carbon atoms such as methyl to tert.-butyl inclusive, especially methyl, ethyl, nand iso-propyl, n-, isoand s-butyl, and the like, more particularly alkyl having 1-3 carbon atoms, and preferably methyl;

Straight and branched chain alkoxy having 1-4 carbon atoms such as methoxy to tert.-butoxy inclusive, especially methoxy, ethoxy, nand iso-propoxy, n-, isoand s-butoxy, and the like, more particularly alkoxy having l-3 carbon atoms, and preferably methoxy and ethoxy; or

-NRR' in which R and R each individually represents Hydrogen or alkyl having l-3 carbon atoms such as methyl to isopropyl inclusive as defined above; especially amino (--NNH and monoand di-methyl amino;

Z represents:

Straight and branched chain alkyl or alkoxy having 1-4 carbon atoms such as methyl to tert.-butyl inclusive as defined above for Y, more particularly alkyl having 1-3 carbon atoms, and preferably methyl and ethyl, and mixtures thereof; and/ or electronegative substitutents such as Halo such as chloro, bromo, iodo and/or fluoro, especially chloro, fiuoro and/or bromo, and more particularly chloro and/ or fluoro;

nitro; cyano;

4 difluoromethyl; trifiuoromethyl; trifluoromethylmercapto, i.e. CF -S; difluorochloromethylmercapto, i.e. CF Cl--S-; trifiuoromethyl sulfonyl, i.e. CF ,-SO trifluoromethyl sulfoxyl, i.e. CF SO; alkyl sulfonyl having 1-4 carbon atoms such as methyl to tert.-butyl inclusive, as defined above, -sulfonyl, especially C alkyl sulfonyl, and more especially methyland ethyl-sulfonyl, i.e. C alkyl-SO dimethylamino sulfonyl, i.e. (CH N-SO and m is a whole number from 1 to 5, especially 1 to 4 or 1 to 3.

The corresponding salts of the instant compounds include the alkali metal salts such as the Na, K, Li, etc. salts, the alkaline earth metal salts such as the Ca, Mg, Ba, Sr, etc. salts, and the amine salts such as secondary and tertiary amine salts such as tri C alkyl and C alkylphenyl amines, e.g. tri same and mixed methyl to butyl -amine, methyl to butyl -phenylamine, etc., especially tri ethyl and ethyl-phenyl amines.

Preferably, X is chloro, bromo, cyano, nitro or azido, Y is C alkyl, C alkoxy, amino or monomethylamino, Z is C alkyl, chloro, fluoro, nitro, cyano, difluoromethyl, difluorochoromethylmercapto, trifluoromethylmercapto, trifluoromethylsulfonyl, C alkylsulfonyl, dimethylaminosulfonyl, and/ or methoxy, with m being 1-5.

In particular, X is chloro or cyano; Y is C alkyl or C alkoxy, Z is methyl, chloro, nitro, trifiuoromethyl, trifiuoromethylmercapto and/or trifluoromethylsulfonyl, with m being 1-5, preferably 1-4 or 1-3.

It will be realized that the process variants [a] and [b] are carried out under practically the same reaction conditions.

As solvents, water and Water-miscible organic solvents are suitable. These include alcohols such as methanol and ethanol, as well as acetic acid, and the like. The organic solvents serve as solubilizer for the methylene component. The reaction is preferably carried out in a pH range of about 4-8. For the bulfering of the mineral acids present in the reaction mixture, bases such as sodium acetate, sodium carbonate, sodium hydroxide, and the like, are added.

The reaction temperatures used are, in general, substantially between about 2 0 to '+30 0., preferably from about 10 to |20 C.

When carrying out the reaction, the starting materials are preferably used in equimolar proportions, the methylene or dicarbonyl component optionally in a small excess. The reaction is, in general, complete after 2-6 hours, it being preferable in many cases to continue stirring for several hours at room temperature. The phenylhydrazones of the present invention are, in general, obtained in crystalline form and can be isolated by filtration from the reaction mixture.

When carrying out process variant [c], the work is accomplished in similar manner. The same solvents and solvent mixtures are used. In this case, however, the pH value is not important. The temperatures used are, in general, substantially between about 0 to C., preferably from about 20 to 70 C.

The phenylhydrazones of the present invention obtained according to the three variants of the process can be converted in the usual manner into their alkali metal salts, alkaline earth metal salts and amine salts. Particularly useful are the sodium, potassium, calcium, magnesium, triethylamine and ethylaniline salts.

The preparation of these solutions is carried out in the usual manner, for example by dissolving the instant phenylhydrazones in organic solvents such as alcohols and adding the appropriate bases. The salts are in most cases sparingly soluble and precipitate, but can also be precipitated with ether. It is also possible to evaporate the solvent.

'Advantageously, the active compound according to the present invention exhibit strong insecticidal and acaricidal activities,with low phytoxicity and relatively low mammalian"toxicity. The active compounds can,'therefore, be used with good results for the control of noxious sucking and biting insects. Diptera as well as mites (Acarina). The effects set in rapidly and are long-lasting.

To the'sucking insects contemplated herein, there belong aphids, such as the green peach aphid (Myzus persicae), the beanaphid (Doralis fabae); scales, such asA'spidiotus hederaefLecanium hesperidum, Pseudow'ccur-maritimus; Thysanoptera, such as Hercinothrips jemoralis; and bugs, such as the beet bug (=Piesma quadrata) and the bed bug (Cimex lectularius), and the like.

With the biting insects contemplated herein, there are classed butterfly caterpillars, such as Plutella maculipennis, Lymantria dispar; beetles, such as granary weevils (Sitophilus granarius), the Colorado beetle (Leptinotarsa decemlineate), but also species living in the soil, such as the Wireworms (Agriotes sp.) and larvae of the cockchafer Melolontha melolontha); cockroaches, such as the German cockroach (Blattella germanica); Orthoptera, such as the house cricket (Gryllus domesticus); termintes, such as Reticulitermes; Hymenoptera, such as ants, and the like. i

The Diptera contemplated herein comprise in particular the flies, such as the vinegar fly (Drosophila melanogaster), the Mediterranean fruit fly (Ceratitis capitata), the house fly (Musca domestica) and mosquitoes, such as. the yellow fever mosquito (Aedes aegypti), and the like.

1n the case of the mites contemplated herein, particularly important are the spider mites (Tetranychidae) such as the two-spotted spider mite (Tetranychus telarius or urticae), the European red mite (Paratetranychus pilosus); blister mites, such as the currant blister mite (Eriophes ribis) and tarsonemids, such as Tarsonemus pallia'us, and ticks, and the like.

If the instant phenylhydrazones are used in the form of their corresponding salts, their effectiveness changes, in general, only extremely slightly.

The active compounds according to the instant invention can be utilized, if desired, in the form of the usual formulations or compositions with conventional pesticidal diluents or extenders, i.e. conventional dispersible carrier vehicles, such as solutions, emulsions, suspensions, emulsifiable concentrates, spray powders, pastes, soluble powders, dusting agents, granules, etc. These are prepared in known manner, for instance by extending the active compounds with conventional pesticidal dispersible liquid diluent carriers and/or dispersible solid carriers optionally with the use of carrier vehicle assistants, e.g. conventional pesticidal surface-active agents, including emulsifying agents and/or dispersing agents, whereby for example in the case where Water is used as diluent, organic solvents may be added as auxiliary solvents. The following may be chiefly considered for use as conventional carrier vehicles for this purpose: dispersible liquid diluent carriers, including inert organic solvents, such as aromatic hydrocarbons, (e.g. benzene, toluene, xylene, etc.) halogenated, especially chlorinated, aromatic hydrocarbons (e.g. chlorobenzenes, etc.), parafiins (e.g. petroleum fractions), chlorinated aliphatic hydrocarbons (e.g. methylene chloride, etc.), alcohols (e.g. methanol, ethanol, propanol, butanol, etc.), amines (e.g. ethanolamine, etc.), ethers, ether-alcohols (e.g. glycol monomethyl ether, etc.), amides (e.g. dimethyl formamide, etc.), sulfoxides (e.g. dimethyl sulfoxides, etc.), ketones (e.g. acetone, etc.), and/or water; as well as dispersible finely divided solid carriers, such as ground natural minerals (e.g. kaolins, alumina, silica, chalk, i.e. calcium carbonate, talc, kieselguhr, etc) and ground synthetic minerals (e.g. highly dispersed silicic acid, silicates, e.g. alkali silicates, etc.); whereas the following may be chiefly considered for use as conventional carrier vehicle assistants, e.g. surface-active agents, for this purpose: emulsifying agents, such as non-ionic and/or anionic emulsifying agents (e.g. poly-. ethylene oxide esters of fatty acids, polyethylene oxide ethers of fatty alcohols, alkyl sulfonates, aryl sulfonates, etc., and especially alkyl aryl-polyglycol ethers, magnesium stearate, sodium oleate, etc.); and/or dispersing agents, such as lignin, sulfite waste liquors, methyl cellulose, etc.

Such active compounds may be employed alone or in the form of mixtures with one another and/or with such solid and/or liquid dispersible carrier vehicles and/ or with other known compatible active agents,-especially plant protection agents, such as other acaricides, insecticides, fungicides, herbicides, bactericides, etc., if desired, or in the form of particular dosage preparations for specific application made therefrom, such as solutions, emulsions, suspensions, powders, paste, and granules which are thus ready for use.

-As concerns commercially marketed preparations, these generally contemplate carrier composition mixtures in which the active compound is present in an amount substantially between about 01-95% by weight, and preferably 05-90% by weight, of the mixture, whereas carrier composition mixtures suitable for direct application or field application generally contemplate those in which the active compound is present in an amount substantially between about 0.001-% or even 2080%, but preferably 0.00 1-5 by weight of the mixture. Thus, the present invention contemplates over-all compositions which comprise mixtures of a conventional pesticidal dispersible carrier vehicle such as (l) a dispersible carrier solid, and/ or (2) a dispersible carrier liquid such as an inert organic solvent and/or water, preferably including a surface-active effective amount of a carrier vehicle assistant, e.g. a surface-active agent, such as an emulsifying agent and/or a dispersing agent, and an amount of the active compound which is effective for the purpose in question and which is generally between about 0.001-%, and preferably 0.00l80%, by weight of the mixture.

The active compounds can'also be used in accordance with the well-known ultra-low volume process with good success, i.e. by applying such compound if normally a liquid, or by applying a liquid composition containing the same, via very effective atomizing equipment in extremely finely dvided form, i.e. mist form, for example by airplane crop spraying techniques. Only a few litres/ hectare are needed, and often amounts up to about 1 quart/acre, preferably 2-16 fluid ounces/acre, are sufficient. In this process it is possible to use highly concentrated liquid compositions with said liquid carrier vehicles containing from about 40 to about 95% by weight of active compound or even the active substance alone, e.g. about 40-100% by weight of the active compound.

Furthermore, the present invention contemplates methods of selectively controlling or combating pests. e.g. arthropods, i.e. insects and acarids, and more particularly, methods of combating at least one of insects and acarids which comprises applying to at least one of correspondingly (a) such insects, (b) such acarids, and (c) the corresponding habitat, i.e. the locus to be protected, a correspondingly combative amount, i.e. an arthropodicidally, especially insecticidally or acaricidally, effective amount of the particular active compound of the invention alone or together with a carrier vehicle as noted above. The instant formulations or compositions are applied in the usual manner, for instance by spraying, atomizing, vaporizing, scattering, dusting, watering, sprinkling, pouring, and the like.

It will be realized, of course, that the concentration of the particular active compound utilized in admixture with the carrier vehicle will depend upon the intended application. Therefore, in special cases it is possible to go above or below the aforementioned concentration ranges.

7 The outstanding activity of the new compounds of the present invention is illustrated without limitation by the following examples:

EXAMPLE 1 Plutella test Solvent: 3 parts by Weight dimethyl formamide Emulsifier: 1 part by weight alkylaryl polyglycol ether.

To produce a suitable preparation of the particular 10 active compound, 1 part by weight of such active compound is mixed with the stated amount of solvent containing the stated amount of emulsifier and the resulting TABLE 1.-PLANI-DAMAGING INSECTS Coneentra- Degree of tion of active destruction compound in percent Active compound in percent after 3 days (A) Cl 0. 2 100 I 9 N 0. 02 0 Qt H CN 01 (known) (41) Cl 0. 2 100 l C N 0. 02 100 H C-O CzHa Cl (51) Cl 0. 2 100 I ON 0. 02 100 H C-O 02H; Cl ll (6r) F C 0 2 10!) CN 0 02 100 I;I-N=C H CO C H; 01

(71) F 0 D. 2 100 CN 0. 02 100 NN=O H C-() 02H; 01

(lz) FgC 0.2 100 I CN 0. 02 100 f 0. 002 100 N-N=C H 0-0 CH3 F 0 (81) 0 F 0. 2 100 CN 0. 02 100 0. 002 80 H C-O 02H; 0 F

(9 Cl 0. 2 100 0. 02 100 Q-I -Nfl: 0. 002 50 H C-CHa 01 II (10 /Cl 00b 2 108 H (J-CH TABLE 1-Coutinuo l IIIIII 7 Concentra- Degree of tion of active destruction compound in percent Active compound in percent after 3 days 7 V (111) 01 0.2 100 V a a l a i r 0. 02 100 Cl NN=O H C-OC2H5 Cl II 0 EXAMPLE 2 A further test was carried out in the same manner as Example 1 and the results are set out below in Table 2.

TABLE 2.-PLANT-DAMAGIN G INSECTS taining the stated amount of emulsifier, and the resulting concentrate is diluted with water to the desired final concentration.

Concentra- Degree of tion of active destruction compound in percent Active compound in percent after 3 days (121) 01 0.2 100 ON 0.02 100 0.002 60 i H CCH: 01 H 0 (13 Cl 0.2 100 CN 0. 02 100 III-N=C J31 H (|.|7-O(CH3)0 H CCH: Cl

01 1IIN=C H a)a Cl (161) CN 0.2 100 o. 02 100 O1- IIIN=C\ H a)s CF; I]

(171) F30 0.2 100 CN 0.02 100 @a I H a)s 01 ll 0 (18 CN 0.2 100 0.02 100 F3C S- --1TIN=O 0.002 90 H ("J-CH3 EXAMPLE 3 Cabbage leaves (Brassica oleracea) are sprayed with r aration o the iven acti om ound until Phaedon larvae test thls p 6p f g 6 p Solvent: 3 parts by weight dimethyl formamide Emulsifier: 1 part by weight alkylaryl polyglycol ether.

To produce a suitable preparation of the particular active compound, 1 part by weight of such active com- 70 dripping wet and then infested with mustard beetle larvae (Phaedon cochleariae).

After the period of time stated in the following table, the degree of destruction of the pests is determined and expressed as a percentage: 100% means that all and 0% pound is mixed with the stated amount of solvent con- 75 means that none of the beetle larvaeare killed. J

The particular active compounds tested, their concentrations, the evaluation time and the experimental results obtained can be seen from the following Table 3:

TABLE 3.PLANTDAMAGING INSECTS Concentra- Degree of tion of active destruction compound in percent Active compound in percent after 3 days (A) CI 0.2 100 1 c N o. 02 0 NN=C H (known) (10:) C1 0. 2 100 CN 0.02 100 C1 lII-N=C l H C-O OH; C1

(42) 5:: Cl 0. 2 100 CN 0.02 100 CI- NN=O (201) .1: CN 0. 2 100 0. 02 100 CI IIIN=C 0.002 50 H C-O CH: F30

H C0 C2H F30 [I (221) C1 0. 2 100 l CN 0. 02 100 H C-OCzH C1 (Z31)..::: CH; 0.2 100 Cl 0.02 100 Qt- H C-OH: CH3

EXAMPLE 4 A further test was carried out in the same manner as Example 3 and the results are set out below in Table 4:

TABLE 4.PLANT-DAMAGING INSECTS Concentration Degree active destruction compound in percent Active compound in percent after 3 days (241) Cl 0. 2 100 CN 0. 02 100 l}I-N=C H C O2-CH Cl (251) G1 0.2 100 I ON 0.02 100 @W H 0 01-0 11 Cl 13 EXAMPLE Tetranychus test I Solvent: 3 parts by weight dimethyl formamide- Emulsifier: 1 part by weight alkylaryl polyglycolether.

5 the preparation of the given active compound is deter- To produce a suitable preparation of the particular active compound, 1 part by weight of such active compound is mixed with the stated amount of the solvent containing the stated amount of emulsifier and the resulting concentrate is diluted with water to the desired final concentration.

Bean plants (Phaseolus vulgaris), which have a height of approximately -30 cm., are sprayed with the prepatrations, the evaluation time and the results obtained can ration of the given active compound until dripping wet.

These bean plants are then heavily infested with spider mites ('Tetranychus telarius) in all stages of development. After --the specified period of time, the eifectiveness of mined by counting the dead mites. The degree of destruction thus obtained is expressed'as a percentage: 100% means that all the spider mites are killed whereas 0% means that none of the spider mites are killed.

The particular active compounds tested, their concenbe seen from the following Table 5:

TABLE 5.PLANT-DAMAGING MIIES Concentra- Degree of tion of active destruction compound in percent Active compound in percent after 8 days (A) CI 0.2 ON 0. 02 0 lTI-N=O I H ON 01 (known) (271) ON 0.2 90 v 0.02 60 NN=C ii 0-0 0 H3 F 30 O H C-O C H:

1 F C 0.2 100 3) 3 CN 0. 02 100 0. 002 50 N-N=C (1 H C-O CH; Fa

(202) CN 0.2 98 0. 02 C1 III-N=O H O-O CH3 F 0 II 0 (222) CI 0.2 CN 0. 02 100 F30- I' IN=O I H 0-0 C2H 01 ll (291)-L'..' I'." T C Ha v '0.2 100 /CI 0. 02 60 1TIN=C B 0-0 0 3 H O IIIN=0 H C-CH3 l I! O (30 Cl 0.2 100 0. 02 98 I 1 H C-O C2H5 TABLE 5.Continued Concentra- Degree of tion of active destruction compound in percent Active compound in percent after 3 days I H C-OH:

| H C-CH G1 I! (32 Cl 0. 2 100 C1 0. 02 100 0.002

(22) FaC 0. 2 100 1 C1 0. 02

| H C-CH; Cl

(33 F 0 0. 0 100 C1 0. 02 60 -1TIN=O l H (J-CH F30 ll 0 (341) F30 0. 2 100 Cl 0. 02 1TIN=C H C-O C1H5 F 0 EXAMPLE 6 A further test was carried out in the same manner as Example 5 and the results are set out below in Table 6;

TABLE 6.PLANT-DAMAGING MITES Coneentra- Degree of tion of active destruction compound in percent Active compound in percent after 8 days (35 Cl 0. 2 100 ON 0. 02 98 C1 1TIN= C\ H (3-011: 1 II H C-CH; 0 Fa ll 17 .EXAMPLE 7.

FaC

1 H CH3 FaC (14) 115 g. 3,5-di (trifluoromethyl)-auiline are diazotized in 400 ml. of 85% H P0 with 157.5 g. of 41% nitrosylsulfuric acid at 10 C. After diazotization, the mixture is diluted with 1000 ml. of water and filtered. This diazoniurn salt solution is added dropwise at 0-10 C., with stirring, to a mixture of 49.5 g. cyanoacetic acid methyl ester in 1000 ml. of 50% acetic acid and 1.1 kg. sodium acetate. In the mixture a pH value of 5 is maintained by further addition of aqueous sodium acetate solution. After completion of the addition of the diazonium salt solution, stirring is continued for 1 hour, and the precipitated product is filtered oil with suction and washed 'with several liters of water. The residue is taken up in methylene chloride, dried over sodium sulfate, and the residue obtained after the methylene chloride has been distilled 01f is recrystallized from white spirit. 136 g. (80% of the theory) of a-cyano-a-carbomethoxy-carbonyl 3,5 bis(trifluoromethyl)-phenylhydrazone are obtained as pale-yellow needles of M.P. 155 C.

EXAMPLE 8 98.5 g. 2,4,5-trichloroaniline are diazotized in 400 ml. of concentrated H 80 (d=1.84) with 157.5 parts of 41% nitrosyl-sulfuric acid at 5-10 C. After diazotization, the mixture is diluted with 1000 ml. of chopped ice and filtered. This diazonium salt solution is then added dropwise at 0-15" 0., with stirring, to a mixture of 57 g. cyanoacetic acid ethyl ester, 250 ml. acetic acid, 1500 ml. of ice water and 2 kg. sodium acetate. A pH value of 4-5 in the mixture is maintained by further addition of sodium acetate. Dilution with 1000 ml. of water is then efiected and stirring is continued for 1 hour. The precipitated product is filtered off with suction and the reaction product is separated from inorganic salts by taking up with methylene chloride. After drying and distilling off of the methylene chloride, 122 g. (76% of the theory) of acyano-u-carboethoxy-carbonyl 2,4,5 trichloro-phenylhydrazone are obtained. Recrystallization from ethanol gives yellow needles of M.P. 133-134 C.

EXAMPLE 9 (I'IJCHa 0 3) 195.5 g. (1 mol) 2-chloro-5-(trifluoromethyl)-aniline are dissolved in 560 g. of concentrated hydrochloric acid. Part of the hydrochloride precipitates. The suspension is added to 1.8 kg. of ice and 1200 ml. of water and diazotization is effected rapidly at 0 C. with 72 g. (1.05 mol) sodium nitrite in 160 ml. of Water. The solution of the diazonium salt is filtered and added dropwise at 05 C. to a mixture of 134.5 g. (1 mol) of a-chloro-acetylacetone in 600 ml. ethanol and 500 g. potassium acetate in 800 ml. of water. During coupling, the pH value was kept to about 6 by the addition of further potassium ace- .tate. The ice cooling is removed and stirring is continued 18 ethanol. 183 g. (61%) a-chloro-a-acetyl-carbonyl-2-. chloro-S-(trifluoromethyl)-phenylhydrazone are obtained as pale yellow crystals of M.P. 151-153 C.

EXAMPLE 1 0 /B r Cl NHN=C C O 2 C 2H5 Cl- -Cl To 400 ml. of phosphoric acid there are added slowly, at -10 C., 157.5 g. nitrosyl-sulfuric acid (42%, D=l.905). 98.2 g. (0.5 mol) 2,4,5-trichloro-aniline are introduced into the mixture at 510 C. Stirring is efiected for 3 hours at 10 C., following by filtration. The diazonium salt solution is then added dropwise to a mixture of 104.5 g. a-bromo-acetoacetic acid ethyl ester, 900 ml. ethanol, 2 kg. ice and 1.1 kg. sodium acetate. The pH value is kept to 5 6 by possible further addition of sodium acetate. After completion of the diazonium salt solution, stirring is continued at 1020 C. for 4 hours, followed by dilution with 4000 ml. of water and suction filtration. The residue on the filter is washed well with water and recrystallized frorn ethanol. 23.5 g. (45%) a-bIOmO-acarboethoxy-carbonyl 2,4,5 trichloro-phenylhydrazone are obtained in the form of a yellowish-grey crystal powder. M.P. -106-1l0 C.

EXAMPLE 1 1 ON NHN=C 29.9 g. (0.1 mol) a-acetyl-e-chloro-carbony1-2-chloro- S-(trifluoromethyl) phenylhydrazone (prepared as described in Example 9) are dissolved in 300 ml. dimethyl formamide and added dropwise at room temperature, with vigorous stirring, to a solution of 7.1 g. (0.11 mol) KCN and 5.6 g. (0.1 mol) KOH in 750 ml. of Water. After completion of the dropwise addition, stirring is continued for 15 minutes, and activated charcoal is added; filtration is efiected and the filtrate is acidified with glacial acetic acid. The precipitate is filtered off with suction, washed with water and dried. 41.0 g. (85%) u-cyano-a-acetylcarbonyl 2 chloro-S-(trifluoromethyl)-phenylhydrazone are obtained in the form of a pale yellow powder which, for purification, can be recrystallized from ethanol. M.P. 114-1l8 C.

EXAMPLE 12 C0 CH3 Cl 34.5 g. (0.15 mol) u-acetyl-u-ch1oro-carbonyl-2-chlorophenylhydrazone, prepared in a manner analogous to Example 9, are dissolved in 500 ml. methanol, and 13.0 g. sodium azide (0.2 mol) are added. The mixture is boiled under reflux for 3 hours, with stirring; filtration from the precipitated sodium chloride is effected and the filtrate is concentrated to about one-fifth of the original volume. After cooling, the precipitated crystals are filtered off with suction and washing is efiected with water, then with cold methanol. 23.5 g. (66%) a-azido-a-acetyl-carbonyl-2-chloro-phenylhydrazone are obtained in the form of a pale brown crystalline substance which, for further purification, can be recrystallized from ethanol. M.P. 121-122 C., decomp.

7-12, the following compounds according to Formula '1 above can be prepared:

TABLE 12 X Y Z M.1?., C

-OC2H5 2- C1, 5-CF3 120-124 CH3 2-01, -CF3 143 0 CH3 2,4,5-013 197 0 C2H5 3,5-(CF3)2 154 -O CzH5 2,6-Cl2, 4-NO2 146-147 --0 CH3 2,6-C12, 4-NO2 159-160 0C2H5 2,5-012, 4-NO2 157 -0 CH3 2,5-C12, 4-NO2 168 -O CzHs 2,4-N02 183-184 0 CzHs 4-SO2DH3 189 O C2115 2-CH3, 6-NO 2 142-146 -OCzH5 2,5-C12, 4-SOzN(CH3)2 160-163 -0 CzHs 2-C1, 4-C F 146 --O C2115 2,6-C12, 4-CF3 116-117 0 CH3 2,6-C12, 4-CF 122 --O C2Hs 2,3,4,5-Cl4 139 -0 C2H5 2-F, 5-CF3 99-101 -0 C2115 2-C F3 117-118 0 CH3 2-C F3 156-157 0 CzHs 3-CF3 1 -0 CH3 3-CF3 1 -O C2H6 4-CF3 135-130 CH3 4-CF3 115 OCzH5 3-CF3, 4-01 151 CH; 3-C F3, 4-Cl 149 0 CH3 2-CF 4-Cl 173-174 --0 CH3 2-N02, 4-CF3 172 -0 CH 2-CN, 5-Cl 169 0 CH 2,4-(CN): 222

-O CH: 3,4-(CN)2 185 0 CH 2-CN, 4-NO2 176-179 --NHCH3 3,5-(CF3): 248

0 CH3 3,5-(CF3)2 133-134 2-CF3, 5-C1 138-139 --0 CzH5 3,4-C12 158-159 -0 CzHs 2-Cl, 5-CF3 114-115 O CgHs 2,6-(CH3): 42-43 CH3 2%}(CF K-salt 235 deeomp:

H2 2,6-(CH3) 2 199 0 CH3 2-C1, 5-01 3 149-151 EXAMPLE 13 In a manner analogous with that described in Examples 7-12, the following compounds according to Formula I above can be prepared:

TABLE 13 X Y Z Mlf C CH: 2-Cl, 5-CF3 114-118 CH3 4-01 228-231 0H3 2-01 117-119 CH3 3-01 188-190 0H3 3,4-012 202-203 CH3 3,5-C12 218-223 0H3 2,4,5-011 138-140 CH3 2-01, 6-CH3 115-118 CH3 2-011 4-01 146-147 CH3 2-CF3, 4-01 109-110 CH3 Z-NOz 199-201 CH3 4-N0z 268-269 0H3 3-01, 4-N0; 222-223 0113 3-NO2, 4-Cl 247-248 CH3 2-NO2, 4,6-012 95-96 CH3 2,5-C1z 4-N0z 176-178 CH3 2;4-(NO 2)2 150-151 0H3 2-0H3, 3-N01 149-150 CH3 2.6-(CH3)2 125-129 CH1 Hm 86-88 CH3 2,6-(C2H5)2 72-73 CH3 4-SO2CH3' 245-247 CH3 v Z-SO2C2H5, 5-01 189-190 a)a 3-01 I 156-157 a03 3,5-012 227-228. 5 (CH3): 3,4-012 216-218 (CHm 201%, 4-01 145-147 X0111): 2,0], 5-01 163-164 x0113); 2-0111. 4-01 173-17 .Yi V .Z M.P.C

C(CHa): 3,5(CF3)2 124-128 C(CH3)3 2,4,5-013 158-161 CH 4-SCF3 -159 CH3 2-SOF3 78-83 CH3 2-SO2CF3 174-175 C(CHs): 4-SCF3 88-89 0 CzHs 2-S02C2H5, 5-CF3 167-168 0 CzH5 2-0 CH3, 4-NO 2, 5-CH3 205 0 C2115 2-0 CH3, 4-C1, 5-CH 149-152 0 C2115 2-CF3, 4-C1 98-100 0 C2115 3,5-C12 131-135 0 CH 2,3,45,6-015 141 0 CH3 2'SO2CZH5, 5-CF3 187-189 OCH3 2-0 H3, 4-N02, 5-0113 190 OCH3 2-0 CH 4-Cl, 5-CH 150-152 0 CH3 3,5-012 -197 0 CH 4-SCF3 128 0 CH3 2-S-CF3 99-100 0 CH 4-SO2CF3 146-150 0 CH 3-CHFz, 4-Cl 136 CH 4-S-C ClFz 96 It will be realized that all of the foregoing compounds contemplated by the present invention possess the desired selective pesticidal, especially arthropodicidal, i.e. insecticidal or acaricidal, properties for combating insects and acarids, and that such compounds have not only a very slight toxicity toward warm-blooded creatures, but also a concomitantly low phytotoxicity.

As may be used herein, i.e. both in the specification and claims, the terms arthropod, arthropodicidal and arthropodicide contemplate specifically both insects and acarids. Thus, the insects and acarids may be considered herein collectively as arthropods to be combated in accordance with the invention, and accordingly the insecticidal and/or acaricidal activity may be termed arthropodicidal activity, and the concomitant combative or effective amount used will be an arthropodicidally efl'ective amount which in effect means an insecticidally or acardicidally eifective amount of the active compound for the desired purposes.

It will be appreciated that the instant specification and examples are set forth by way of illustration and not limitation, and that various modifications and changes may be made without departing from the spirit and scope of the present invention which is to be limited only by the scope of the appended claims.

What is claimed is: t

1. A compound selected from the group consisting of a phenylhydrazone having the formula in which Y is selected from the group consisting of alkyl and alkoxy having 1-4 carbon atoms, each individual Z is selected from the group consisting of methyl, trifluoromethyl, trifluoromethyl mercapto, chloro, nitro and cyano, and m is a whole number from 1-3; and the corresponding salt thereof selected from the group consisting of alkali metal, alkaline earth metal and amine salt. '2. Compound according to claim' 1 wherein each Z individually is selected from the group consisting of chloro and trifluoromethyl.

3. Compound according to claim 1 wherein such compound 'is u-cyano-a-carbomethoxy-carbonyl-3,5-bis(trifluoromethyl)-phenylhydrazone having the formula 4. Compound according to claim 1 wherein such compound is a-cyano-at-acetyl-carbonyl-2-chloro-5-(trifluoromethyl)-phenylhydrazone having the formula CO CH: C1

5. Compound according to claim 1 wherein such compound is a-cyano-a-carboethoxy-carbonyl-2,4,5-trich1oro- -phenylhydrazone having the formula References Cited UNITED STATES PATENTS 3,150,151 9/1964 Urbschat et a1. 26 0-465 3,213,124 10/1965 Sheppard 260465 CHARLES B. PARKER, Primary Examiner C. F. WARREN, Assistant Examiner U.S. Cl. X.R.

4 PUNITED STATES PATENT OFFICE CERTIFICATE OF CUBRECTION Patent No. 3,641,098 paged February a, 1972 lnventofls) Kerl-Heinz Buchel, 'et. a1. i

It is certified that error appears in the above ident1fied patent and that said Letters Patent are hereby corrected as shown below:

Col. 1, line 30 "phenylhyazones" should be --phe r 1ylhyc 1razones-fe01; 1, iine 54 "cyan" should be -cyan'o-- 7 Col. 3 line 62' n( N 2 n hould l e ------(--NH2) I Col. 5, line 23 "termintes" 'shofil-d be -termit es-- Col. 19, Table 12, line 10 of ""z" cam -S0 -DH shouldebe --'4-so Signed and sealed thie 24th day of April 1973.,

(SEAL), I LAtteSt: I H v i :l J

EDWARD M.FLETqmsR,JR. Z ROBERT GOTI'SCHAL-K Attesting offlcer Commissioner of Patents 

